A novel syndrome of abnormal striatum and congenital cataract: Evidence for linkage to chromosomes 11

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作者： Al-Owain,M. ^[1] ; Al-Zahrani,J. ^[2] ; Al-Bakheet,A. ^[3] ; Abudheim,N. ^[4] ; Al-Younes,B. ^[5] ; Aldhalaan,H. ^[6] ; Al-Zaidan,H. ; Colak,D. ; Almohaileb,F. ; Abouzied,M. ; Al-Fadhli,F. ; Meyer,B. ; Kaya,N.

作者单位： Department of Neurosciences, Riyadh, Saudi Arabia ^[1] Department of Biostatistics, Epidemiology and Scientific Computing, Riyadh, Saudi Arabia ^[2] Department of Medical Genetics, Riyadh, Saudi Arabia ^[3] Department of Pediatrics, Maternity and Children Hospital, Al-Madinah, Saudi Arabia ^[4] Department of Radiology, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia ^[5] Department of Genetics, Riyadh, Saudi Arabia ^[6]

关键词 Affymetrix 10K mapping assay Affymetrix 6.0 mapping assay Cataract Chromosome 11 Dysmorphia Genome-wide scan Linkage Mental retardation Microcephaly Putamen

发布时间 2018-06-23

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